Ohtsuki H, Haebara H, Takahashi K, Midorikawa O, Tomoyoshi E, Torii S, Miura K
Neuropediatrics. 1981 Aug;12(3):279-86. doi: 10.1055/s-2008-1059658.
A Japanese girl aged 19 months had generalized convulsions, agenesis of the corpus callosum, peculiar chorioretinopathy, scoliosis and marked retardation of psychomotor development. Pathological investigation revealed polymicrogyria, cortical heterotopias, disorganization of the cerebellar cortex. In ocular histopathology, lacunae were composed of hypo- or depigmented zones of the retinal pigment epithelium accompanied with dispersion of pigments into the rod and cone layer. Coloboma of the optic nerve was also evident. There was no evidence of inflammation or pathogenic organisms.
一名19个月大的日本女孩出现全身性惊厥、胼胝体发育不全、特殊的脉络膜视网膜病变、脊柱侧弯以及精神运动发育明显迟缓。病理检查显示多小脑回、皮质异位、小脑皮质结构紊乱。眼部组织病理学检查发现,视网膜色素上皮的低色素或无色素区形成腔隙,同时色素分散至视杆和视锥层。视神经缺损也很明显。没有炎症或病原体的证据。